2378 results about "Aromatic hydrocarbon" patented technology

The invention provides a method for determining hydrocarbon components in mixed aromatic hydrocarbons by using comprehensive two-dimensional gas chromatography-mass spectrometry. The method comprises the following steps: optimizing a target function to make a chromatographic peak signal obtained by a separation model accord with a chromatographic separation process mechanism, fully utilizing complementary information of chromatography and mass spectrometry, improving separation precision, and guiding analysis of complex aliasing peaks; analyzing overlapped chromatographic peaks determined by principal component analysis by adopting the established separation model to obtain a chromatographic peak signal representing a single component after separation, and matching the chromatographic peak signal with a corresponding mass spectrum; in combination with a single chromatographic peak signal and a mass spectrum obtained through separation, according to characteristic fragments and chromatographic retention time in the mass spectrum, component types corresponding to chromatographic peaks are judged, and characterization of the composition of the mixed aromatic hydrocarbon is achieved; a separated single chromatographic peak is subjected to quantitative analysis, the content of each component is calculated by adopting an external standard method in contrast with a standard curve, a quantitative result of the mixed aromatic hydrocarbon sample is obtained, and the measurement precision of the mass fraction of each hydrocarbon component is improved.

The invention relates to the technical field of hydrogen storage and release, and discloses a cyclic hydrogen storage and release system based on aromatic cycloalkane reaction, which comprises a hydrogenation reaction unit, a dehydrogenation reaction unit, a gas-liquid separation and compression unit and an adsorption and purification unit which are sequentially connected through pipelines, the hydrogenation reaction unit, the dehydrogenation reaction unit and the gas-liquid separation and compression unit are respectively connected with the heat exchange unit; the hydrogen storage function and the hydrogen desorption function are integrally designed, the microwave heat supply dehydrogenation reactor is designed for the dehydrogenation reaction link with high energy consumption, and compared with the prior art, the microwave heat supply dehydrogenation reactor has the advantages that the heat transfer resistance is reduced, the reaction efficiency is improved, and the energy loss is reduced. The designed gas-liquid separation and adsorption purification technology is coupled, only one compressor is used in the whole process, the purification process is effectively simplified, the operation is simple and convenient, the equipment cost and the hydrogen purification cost are reduced, and the hydrogen yield and the hydrogen storage carrier cyclic utilization rate are improved. The system has the advantages of high hydrogen storage and release efficiency, small system size, high mobility and the like.

The invention discloses a method for preparing fuel from waste polyolefin through noble-metal-free low-temperature aromatization, which comprises the following steps: in the atmosphere of synthesis gas, carrying out catalytic cracking on polyolefin serving as a raw material by adopting a binary mixed catalytic system to obtain aromatic hydrocarbon; the binary mixed catalytic system comprises Zr-ZnO and a molecular sieve; the catalytic cracking temperature is less than or equal to 300 DEG C. According to the low-temperature aromatization method disclosed by the invention, methanol is generated in situ through the synthesis gas, and the methanol and olefin generated by polyolefin cracking are subjected to Prins reaction, so that the aromatization reaction can be realized at the pyrolysis temperature far lower than that in the prior art, precious metals are not needed, the additional value and the application range of a plastic recovery product are greatly enhanced, and the method is suitable for industrial production. And the cost of the recovery process is reduced.

The invention relates to an aromatic hydrocarbon isomer adsorbent containing a modified X-type molecular sieve. The outer surface area of the modified X-type molecular sieve is 9.5-19m < 2 > / g, and the sum of the pore volume of mesopores and the pore volume of macropores is 6%-18% of the total pore volume. The p-xylene adsorbent comprises 88-95% by mass of a modified X-type molecular sieve, 4-11% by mass of a crystal transformation X-type molecular sieve and 1-3% by mass of a matrix. The invention also relates to a preparation method of the adsorbent and application of the adsorbent in adsorption separation of p-xylene from mixed C8 aromatic hydrocarbons.

The invention provides a Pt-Sn bimetallic catalyst and a preparation method and application thereof.The preparation method comprises the steps that 1, a Y molecular sieve is placed in a mixed solution of KOH and methyl alcohol, centrifugation and washing are conducted till the Y molecular sieve is neutral after stirring, drying and roasting are conducted, and a non-acid KY molecular sieve is obtained; the silica-alumina ratio of the Y molecular sieve is 3-100; 2) taking the non-acidic KY molecular sieve as a carrier, and loading Sn by adopting an atomic layer deposition technology to obtain a Sn-modified non-acidic KY molecular sieve; and 3) loading Pt by using the Sn-modified non-acidic KY molecular sieve as a carrier and adopting an atomic layer deposition technology to obtain the Pt-Sn bimetallic catalyst. According to the preparation method provided by the invention, spatial distribution of Pt and Sn is accurately regulated and controlled by combining an atomic layer deposition technology, so that the electronic state of Pt species is adjusted, alkane is promoted to be dehydrogenated into an olefin intermediate, and the aromatization catalytic activity and the aromatic hydrocarbon selectivity of alkane are improved.

The invention provides a surface treatment method of a lithium metal pole piece. The invention relates to a surface treatment method of a lithium metal pole piece, which comprises the following steps: reacting the lithium metal pole piece in an organic solvent solution of an aromatic hydrocarbon complexing agent in an inert atmosphere, then taking out the lithium metal pole piece, and cleaning; placing the cleaned lithium metal pole piece in reactive gas for reaction to obtain a modified lithium metal pole piece; wherein the aromatic hydrocarbon complexing agent is a complexing agent which can be subjected to a complexing reaction with lithium, and the reactive gas comprises an oxidizing gas. The original inorganic layer with rough surface appearance and non-uniform component distribution of the lithium metal pole piece is changed into the flat lithium-containing inorganic layer, so that the impedance is reduced, and the service life of the battery is prolonged.

The invention discloses a perovskite precursor solution containing substituted aromatic ring group sulfonic acid, which comprises a perovskite material, an additive and an organic solvent, the additive is aromatic ring group sulfonic acid with a substituent group or a salt thereof, the aromatic ring is a benzene ring, a naphthalene ring or a pyrene ring, and the substituent group is one or more of H, halogen, C1-C4 alkenyl and C1-C4 alkyl. Polycyclic aromatic hydrocarbon (such as benzene, naphthalene and pyrene) is used as a framework, one sulfonic acid group instead of a sulfonyl group is introduced, and uncoordinated type defect passivation is realized through bonding with Pb < 2 + >; meanwhile, the electron push-pull characteristic of the substituent group is utilized, the Lewis acid-base amphoteric property is exerted, passivation of various types of defects is achieved, anchoring and passivation of multiple sites are achieved, the defects of the perovskite active layer can be remarkably reduced, non-radiative recombination can be reduced, and the performance and stability of the prepared perovskite solar cell in the large-scale preparation process are further improved.

The invention is applicable to the technical field of eutectic materials, and provides an organic macrocyclic aromatic hydrocarbon-based eutectic material and a preparation method and application thereof, the eutectic material is a metastable material EtLP6-F4TCNQ alpha, and is prepared by taking oblique tower aromatic hydrocarbon as a subject and electron-deficient 2, 3, 5, 6-tetrafluoro-7, 7, 8, 8-tetracyanodimethyl p-benzoquinone as an object, and carrying out co-crystallization on the oblique tower aromatic hydrocarbon and the 2, 3, 5, 6-tetrafluoro-7, 7, 8, 8-tetracyanodimethyl p-benzoquinone to obtain the organic macrocyclic aromatic hydrocarbon-based eutectic material. And carrying out mechanical grinding on 2, 3, 4, 5, 6, 8-tetracyanodimethyl p-benzoquinone. According to the method, two or more organic molecules are directly mixed and induced to form the eutectic structure through simple mechanical grinding operation, the method is efficient, low in cost and easy for large-scale production, the eutectic material with the metastable structure is prepared, and the metastable structure shows higher sensitivity and faster response speed in gasochromic detection.

The invention relates to the technical field of fluorite flotation reagents, in particular to a preparation method of a fluorite flotation collecting agent. The specific preparation method comprises the following steps: carrying out sulfonation reaction on sulfuric acid and benzene to obtain sulfonation reaction liquid; the method comprises the following steps: by taking oleic acid or acid oil as a raw material, adding sulfonation reaction liquid at 10-20 DEG C, and carrying out stirring reaction; adding alkali liquor to carry out neutralization reaction, controlling the temperature to be less than or equal to 80 DEG C, and adjusting the pH value to be 7-8; and a water phase is separated and removed, and a mixture containing oleate, sulfated oleate, hydroxyl oleate and stearic acid benzene sulfonate is obtained and serves as the fluorite flotation collecting agent. By controlling the proportion of sulfuric acid to benzene and adding oleic acid, on the basis of reducing product benzene residues, the collecting capacity is improved, good selectivity is achieved, and the problem of aromatic hydrocarbon residues existing in a flotation collecting agent prepared from aromatic hydrocarbons such as benzene as raw materials is solved.

The application discloses a thickened oil viscosity reducer for a main viscosity contribution component of colloid and a preparation method thereof. The thickened oil viscosity reducer comprises the following components in percentage by weight: diethylene glycol methyl ether 25-35%, propylene glycol formate 15-25%, dispersant 5-8%, chelating agent 2-4%, anti-coking agent 0.5-1%, anti-swelling agent 1-2% and corrosion inhibitor 1-2%; and the balance is water. The application is a polar + non-aromatic hydrocarbon solvent system; completely avoids high-risk substances such as nonylphenol polyoxyethylene ether, petroleum sulfonate sodium and organic chlorine; is designed in pertinence and can effectively inhibit metal-induced asphaltene bridging; can withstand working conditions from normal temperature to 250 DEG C and up to 300 DEG C; thermal stability is significantly enhanced, and residual carbon after aging is lower than 8%; viscosity reduction efficiency is higher; the system is more stable, flexible in compounding and suitable for field construction.

The invention relates to a PVB (Polyvinyl Butyral) film for PDLC (Polymer Dispersed Liquid Crystal) dimming glass, a preparation method and the PDLC dimming glass, and belongs to the technical field of dimming glass. The PVB film for the PDLC dimming glass comprises PVB resin and a plasticizer, at least one end group of the plasticizer is a benzoate group, and the plasticizer belongs to benzoate. Through molecular structure design, the main chain of the plasticizer can be a polyether type [-CH2-CHY-O-] n chain segment or a polyol skeleton, and meanwhile, benzoate groups or specific end group structures (such as branched chain alkyl, aromatic hydrocarbon and the like) are introduced, so that the interaction (such as hydrogen bond damage, dipole interaction, pi-pi accumulation and the like) between the plasticizer and PVB resin is enhanced, and the plasticizer can be used for preparing PVB resin. By introducing structures such as branched chains and aromatic rings, the steric hindrance and rigidity of molecules are greatly improved, and migration and precipitation phenomena of the plasticizer in the PVB film are effectively inhibited.

The invention discloses a metal modified molecular sieve catalyst and a preparation method and application thereof. The catalyst is a metal-loaded molecular sieve which is modified by post-treatment after a metal component is loaded on the molecular sieve; the molecular sieve is selected from at least one of H-ZSM-5, H-Beta, H-ZSM-35, H-MOR, H-MCM-22, H-ZSM-11 and H-ZSM-22, and the molecular sieve is selected from at least one of H-ZSM-5, H-Beta, the metal is loaded on the molecular sieve through ion exchange and / or impregnation; the post-treatment modification is selected from at least one of heating treatment, water vapor treatment and silanization treatment. The metal component of the catalyst can catalyze dehydrogenation reaction and carbon dioxide activation, the molecular sieve component provides a substance diffusion channel and an acid center, and post-treatment modification can regulate the distribution of the molecular sieve acid center and improve the hydrothermal stability of the catalyst. The catalyst can efficiently promote the coupling reaction of cycloalkane and carbon dioxide, the selectivity of aromatic hydrocarbon reaches 90% or above, and the conversion rate of carbon dioxide reaches 20% or above.

The invention belongs to the technical field of organic waste gas adsorption treatment, and particularly relates to enhanced activated carbon for organic waste gas and a preparation method thereof. The invention discloses a modified coconut shell activated carbon adsorbent, which is prepared from the following raw material components: coconut shell activated carbon, Mn (NO3) 2.4 H2O, Ce (NO3) 3.6 H2O, 3-glycidoxypropyltrimethoxysilane, organic affinity silane and a water repellent agent. According to the method, a Mn-Ce mixed oxide core is generated in situ in an inner hole through equivalent-volume impregnation and staged heat treatment, and is used for digesting oxygen-containing organic matters, adsorbing intermediates and keeping the hole channel clean; forming a silica anchoring layer on the surface of the activated carbon by using GPTMS, and carrying out co-condensation on the silica anchoring layer and organic affinity silane to obtain an organic affinity interface matched with aromatic hydrocarbon and non-polar VOC (Volatile Organic Compounds) without blocking holes; an ultra-thin hydrophobic layer is formed at the tail end through polycondensation of low-dosage hydrophobic silane, moisture permeation is reduced, and meanwhile, an organic small molecule diffusion channel is reserved; and the pore structure is effectively protected by adopting a water / alcohol system and low-temperature curing in the whole process.

The invention belongs to the technical field of waste plastic treatment, and particularly relates to a method for preparing light aromatic hydrocarbon through catalytic pyrolysis of waste polyolefin plastic. According to the invention, a microporous molecular sieve ZSM-5 is coated in an ordered mesoporous layer SBA-15 by using a super-dilute liquid phase coating method, so that the coated catalyst ZSM-5-coated SBA-15 with the packaging thickness of 60-185 nm is prepared. The coated catalyst has an ordered mesoporous encapsulation layer, and can be pre-cracked and enrich plastic pyrolysis volatile components in the reaction, so that the mass transfer rate is increased, the generation of light aromatic hydrocarbons is promoted, the generation of macromolecular chain hydrocarbon substances in the catalytic pyrolysis process is inhibited, and the efficient preparation of light aromatic hydrocarbons by catalytic pyrolysis of waste polyolefin plastics is realized. Compared with the traditional ZSM-5, when the packaging thickness of the ZSM-5-coated SBA-15 is 90nm, the yield of light aromatic hydrocarbon is 31.02 wt.%, the amplification is up to 49.14%, and meanwhile, the heavy chain hydrocarbon byproduct is reduced by 42.17%.

The invention provides a high-performance concrete anticorrosive paint and a preparation method of a coating, and relates to the technical field of building materials and corrosion prevention. The coating is composed of a component A and a component B, the component A comprises epoxy resin, a composite solvent, an organic solvent, a dispersant, fumed silica and a leveling agent, and the component B comprises an epoxy hardener, a conductive polymer dispersion liquid and an organic solvent. The composite solvent is formed by compounding one or more of orthotitanate, phosphate and orthosilicate with an ester, ketone, alcohol, aromatic hydrocarbon, aliphatic hydrocarbon or ether organic solvent. The preparation method of the anticorrosive coating comprises the following steps: preparing the component A and the component B, mixing to form a coating, applying the coating to the surface of concrete, and curing. The coating is compact in structure and strong in adhesive force, can obviously improve the durability and corrosion resistance of concrete in extreme environments such as high salinity and high acid, and is particularly suitable for infrastructure protection in coastal and heavy corrosion industrial areas.

The invention relates to an MPC control method of an industrial aromatic hydrocarbon combination unit. The MPC control method comprises the following steps: establishing a model of the industrial aromatic hydrocarbon combination unit; a state space model is adopted to describe: # imgabs0 # design parameter identification algorithm, and parameters A, B and C of the model are accurately estimated; designing an MPC controller based on the established state space model; a coordination control mechanism of the MPC is designed, the industrial aromatic hydrocarbon combination device is divided into a plurality of subsystems, each subsystem is controlled by a local MPC controller, and the subsystems are coordinated through information interaction; by improving the accuracy and adaptability of the model, optimizing a parameter identification algorithm and designing an effective coordination control mechanism, accurate control of the industrial aromatic hydrocarbon combination unit is realized, the production efficiency, the product quality and the stability are improved, and the energy consumption is reduced.

The present application relates to a kind of green olefin removal method completely replacing clay, which comprises under liquid phase continuous hydrotreating conditions, first, reforming generated oil is mixed with hydrogen through high-efficiency mixer, hydrogen is mixed with reforming generated oil intensively and quickly, and saturated hydrogen-dissolved reforming generated oil is obtained, the saturated hydrogen-dissolved reforming generated oil is sent into first hydrogenation reactor, first contact with nickel-containing catalyst, and the reaction product is then introduced into second hydrogenation reactor, and contact with noble metal-containing catalyst.Reformate is treated by olefin removal, and the product obtained mainly contains benzene, toluene, xylene and other aromatic hydrocarbons, the bromine index of which is less than 20 mgBr / 100g oil, and the loss of aromatic hydrocarbons is less than 0.1wt%.

The invention discloses a lithium metal battery and a modified cathode thereof. The preparation method of the negative electrode comprises the following steps: providing a clean metal lithium sheet; providing, as a treatment agent, an organic solution containing a compound of general formula R-A-X, where R is an aliphatic hydrocarbon group or an aromatic hydrocarbon group, A is at least one metal selected from the group consisting of Mg, Al, Zn, K, Na, Ca, Sn, In and Fe, and X is at least one halogen selected from the group consisting of F, Cl, Br, I and At; and carrying out surface chemical treatment on the metal lithium sheet by using a treating agent under a protective atmosphere to prepare the negative electrode. The interface layer is formed on the surface of the lithium metal, so that on one hand, the lithium alloy contained in the interface layer can remarkably promote rapid transmission of lithium ions and effectively inhibit growth of lithium dendrites; on the other hand, the contained halide can be dissolved in the electrolyte in the cycle process of the battery to react with dead lithium generated by the lithium metal negative electrode to generate active lithium, so that the performance of the battery is remarkably improved.

The present invention provides a mechanically interlocking epoxy resin polymer, a preparation method, and an application thereof. The raw materials for preparing the mechanically interlocking epoxy resin polymer include pillar aromatic hydrocarbon daisy chain polyurethane, epoxy resin, and a crosslinking agent. In the present invention, the pillar aromatic hydrocarbon daisy chain polyurethane, epoxy resin, and crosslinking agent are ring-opening polymerized to form a mechanically interlocking polymer containing a daisy chain. The crosslinking agent crosslinks the polymer containing the daisy chain into a network. The prepared mechanically interlocking epoxy resin polymer has dynamic properties, which mainly come from the host-guest recognition effect of the pillar aromatic hydrocarbon and triazole. This dynamic property can improve the mechanical properties and energy dissipation of traditional epoxy resins, allowing the epoxy resin to withstand greater stress, enhancing its toughness, and promoting maximum elongation and ductility without sacrificing the mechanical strength of the polymer.

A method for producing an aromatic heterocycle-substituted difluoroacetic acid derivative having a partial structure represented by the formula (III), by reacting an N-oxido aromatic heterocyclic compound having a partial structure represented by the formula (I) with tetrafluoroethylene in the presence of a compound represented by the formula (II): R—YH, in a solvent selected from an aromatic hydrocarbon solvent, an ester solvent and an ether solvent:

The invention belongs to the technical field of biomass energy utilization, and particularly relates to a method for improving the selectivity of light aromatic hydrocarbon in a biomass product through catalytic pyrolysis of a zeolite molecular sieve catalyst. The content of medium-strong acid sites in the zeolite molecular sieve catalyst is found to have relatively strong positive correlation with the selectivity of light aromatic hydrocarbons prepared during catalytic pyrolysis of biomass, so that when the zeolite molecular sieve catalyst is used for catalytic pyrolysis of biomass, the content of the medium-strong acid sites in the zeolite molecular sieve catalyst can be increased by increasing the proportion of the medium-strong acid sites in the zeolite molecular sieve catalyst; the selectivity of light aromatic hydrocarbon in the catalytic pyrolysis product is improved.

The invention discloses an intelligent catalytic thermal cracking reaction system and method for complex mixed waste plastics, and belongs to the technical field of waste plastic resourceful treatment. The system comprises a feeding device, a high-pressure multi-section cracking reaction kettle, a spraying type heat exchange temperature control system, a heating system, a sensing and analyzing unit, an intelligent control system and a product condensation separation and utilization unit, the method specifically comprises the following steps: (1) pretreating and feeding raw materials; (2) multi-section temperature control cracking reaction; (3) intelligent feedback control; (4) the catalyst has a synergistic effect; and (5) product separation and recovery. According to the invention, a unique spraying type high-pressure multi-section temperature control system is combined with intelligent control of a rate matching algorithm, so that efficient, directional and stable cracking of complex mixed waste plastics is realized, the yield of high-value products such as light olefins, aromatic hydrocarbons and the like is remarkably improved, byproduct residues and energy consumption are reduced, and long-term continuous operation is realized.

The utility model relates to a liquid hydrogen storage system which comprises an integrated hydrogen storage device and a hydrogen storage medium, the integrated hydrogen storage device comprises a liquid storage tank for storing a hydrogen storage medium, a gas storage tank for storing hydrogen, a reactor connected with the output ends of the liquid storage tank and the gas storage tank, a condenser connected with the reactor, a gas-liquid separator connected with the output end of the condenser, a gas compressor and a gas buffer tank, and one or more unsaturated aromatic hydrocarbons or heterocyclic unsaturated compounds with a saturated vapor pressure of more than 1 kPa and a temperature of 20 DEG C. The gas-phase storage medium of the liquid hydrogen storage system sequentially passes through the condenser, the gas-liquid separator, the gas compressor and the gas buffer tank, so that a hydrogen pressurizing, cooling and refluxing process is realized, a liquid hydrogen storage material can be effectively recycled, and the purity of hydrogen can be ensured.

The invention provides an optimization method and system for a biomass catalytic pyrolysis process, belongs to the crossing field of chemical engineering and artificial intelligence, and aims to solve the problem of collaborative optimization of the yield of multiple competitive aromatic hydrocarbon products. The method comprises the following steps: acquiring a data set containing input parameters and corresponding to multiple target aromatic hydrocarbon yields; training a machine learning prediction model based on the data set; integrating the model with a multi-objective optimization algorithm; the model is called through an algorithm to conduct iterative optimization, a Pareto optimal solution set is obtained with the aim of optimizing the yield of multiple aromatic hydrocarbons at the same time, and the solution set comprises multiple sets of optimized input parameter combinations. According to the method, efficient global optimization can be realized, multi-scheme decision support is provided, and the research and development cost is reduced.

The invention discloses a long-afterglow material based on waste PET and a preparation method and application thereof.Organic luminescent substance crown alkene serves as luminescent molecules and is fused and doped into recycled waste PET, the waste PET is upgraded and reconstructed into a persistent luminescent polymer element, PET macromolecular chains are folded front and back to form regular lamellas, and the lamellas are uniformly distributed on the surface of the waste PET, so that the long-afterglow material based on the waste PET is obtained. Excitons are stabilized, and oxygen in the atmosphere is prevented from being quenched. Due to the planar and rigid structure of the polycyclic aromatic hydrocarbon, intramolecular movement can be inhibited, so that non-radiative decay channels are reduced, and the ultra-long afterglow effect is realized. According to the long-afterglow material, pollution of waste materials is reduced, upgrading and recycling of resources are achieved, upgrading and recycling steps are simple and convenient, cost is low, the preparation process is easy to scale, economical and efficient, and the long-afterglow material has good industrial popularization prospects and has important application value in the technical field of plastic upgrading and recycling.

The invention provides a continuous process for preparing aromatic hydrocarbon by supercritical carbon dioxide hydrogenation, which comprises the following steps: 1) adding a reaction liquid containing a solvent and a catalyst into a reaction kettle, spraying supercritical carbon dioxide and hydrogen into a reactor by adopting a Venturi ejector, and contacting with the catalyst in the reaction kettle to react; (2) after the reaction in the step (1), the gas in the reactor is sequentially subjected to primary condensation and secondary condensation to respectively condense the solvent and the water, the solvent of the primary condensation returns to the reaction kettle, the water of the secondary condensation is discharged, and the gas after the secondary condensation sequentially passes through an absorption tower and a desorption tower to capture non-aromatic hydrocarbon, the residual gas is used as recycle gas and returns to the Venturi ejector to enter the reaction kettle; and (3) pressurizing the reaction liquid discharged from the reaction kettle after the reaction in the step (1) through a circulating pump, feeding the reaction liquid into a heat exchanger to remove reaction heat, dividing the reaction liquid subjected to heat exchange into two streams through a cross-flow filter, feeding one stream of penetrating fluid into a rectification device, and feeding the other stream of concentrated liquid back to the reaction kettle for continuous reaction.

The invention provides an efficient technological method and system for preparing aromatic hydrocarbon through CO2 hydrogenation. The process method comprises the following steps: 1) mixing feed gas containing CO2 and H2 with recycle gas to obtain a mixture flow, and carrying out first-stage reaction on the mixture flow after heat exchange heating to obtain a first-stage reaction product; 2) performing heat exchange and separation on the primary reaction product to obtain a water phase, a gas phase and an oil phase, discharging the water phase out of the system, compressing most of the gas phase to obtain continuous circulating gas, and circulating the circulating gas back to the step 1) to continue the reaction; a small part of gas phase is discharged as purge gas; 3) distilling out light hydrocarbon from the top of the tower by rectifying the oil phase to obtain aromatic hydrocarbon-rich oil from a tower kettle; 4) heating the light hydrocarbon and then carrying out secondary reaction to obtain a secondary reaction product; and 5) carrying out heat exchange and separation on the secondary reaction product to obtain a gas-phase product and a liquid-phase product, discharging the gas-phase product as purge gas, and circulating the liquid-phase product back to the light component removal tower for rectification and separation to obtain aromatic hydrocarbon-rich oil. The first-stage reaction realizes high per-pass conversion of CO2, and the two-stage reaction is coupled to realize high selectivity of aromatic hydrocarbon.

The utility model discloses a hydrogen storage and supply device and a hydrogen fuel cell heat and power cogeneration system, and relates to the technical field of fuel cells. The hydrogen storage and supply device realizes normal-temperature and normal-pressure storage of hydrogen on the basis of a liquid organic matter hydrogen storage technology, and the principle is that hydrogen storage is realized by virtue of reversible reaction and hydrogenation reaction of unsaturated liquid organic matters such as olefin, alkyne or aromatic hydrocarbon and hydrogen, and hydrogen release is realized by virtue of dehydrogenation reaction. According to the liquid organic matter hydrogen storage technology, the hydrogen storage density is 5%-10%, and the hydrogen storage amount is large; and the hydrogen storage carrier is a liquid organic matter, normal-temperature and normal-pressure transportation can be achieved, convenience and safety are achieved, the requirement for the hydrogen liquid tank is low, and hydrogen leakage is basically avoided during transportation. And during dehydrogenation reaction, the temperature required by hydrogen desorption is low, the energy consumption is low, the hydrogen desorption rate is adjustable, and the hydrogen desorption device can be adapted to various hydrogen fuel cells. The hydrogen fuel cell heat and power cogeneration system collects and utilizes the lost heat of the cell, so that the comprehensive utilization rate of the hydrogen fuel cell is improved.

The invention provides an electrolyte suitable for a lithium negative electrode or a negative-electrode-free lithium battery, a lithium metal battery and a negative-electrode-free battery. The electrolyte comprises a solvent, a diluent and fluorine-containing lithium salt, wherein the solvent is selected from one or more of a linear ether solvent, a cyclic ether solvent and a siloxane solvent, and the linear ether solvent, the cyclic ether solvent and the siloxane solvent optionally have cyano substituent groups; the diluent is selected from one or more of a group consisting of fluoro aromatic hydrocarbon and fluoro alkane. The specific solvent and diluent are used, and the additive is further used, so that the electrochemical stability window and the capacity retention ratio and the lithium deposition efficiency of the battery are remarkably improved.

The present application relates to the technical field of ZSM-5 molecular sieve preparation, and provides a high-crystallinity aluminum-rich ZSM-5 molecular sieve, a preparation method and application thereof.The preparation method of the high-crystallinity aluminum-rich ZSM-5 molecular sieve provided by the present application realizes the skeleton composition control of the ZSM-5 molecular sieve by adding a second aluminum source and then performing secondary crystallization, solves the technical bottleneck that it is difficult to directly synthesize the high-crystallinity aluminum-rich ZSM-5, breaks through the lower limit of the Si / Al ratio phase region of the artificial in-situ synthesis of the molecular sieve, effectively controls the crystal parameter and improves the production efficiency, realizes the precise construction of the high-crystallinity aluminum-rich ZSM-5 molecular sieve, and thus enhances the micropore crystallinity of the molecular sieve, optimizes the acid distribution, greatly enriches the metastable surface active acid center distribution of the molecular sieve, and has good aromatic hydrocarbon conversion performance.